A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5997637



Internal ID21906980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:576901..576952hg38UCSC Ensembl
chr4:570690..570741hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17548630
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5997637
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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